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Many QTLs with minor additive effects are associated with a large difference in growth between two selection lines in chickens

  • LINA JACOBSSON (a1), HEE-BOK PARK (a2), PER WAHLBERG (a2), ROBERT FREDRIKSSON (a3), MIGUEL PEREZ-ENCISO (a4) (a5), PAUL B. SIEGEL (a6) and LEIF ANDERSSON (a1) (a2)...
Abstract

Two growth-selected lines in chickens have been developed from a single founder population by divergent selection for body weight at 56 days of age. After more than 40 generations of selection they show a nine-fold difference in body weight at selection age and large differences in growth rate, appetite, fat deposition and metabolic characteristics. We have generated a large intercross between these lines comprising more than 800 F2 birds. QTL mapping revealed 13 loci affecting growth. The most striking observation was that the allele in the high weight line in all cases was associated with enhanced growth, but each locus explained only a small proportion of the phenotypic variance using a standard QTL model (1·3–3·1%). This result is in sharp contrast to our previous study where we reported that the two-fold difference in adult body size between the red junglefowl and White Leghorn domestic chickens is explained by a small number of QTLs with large additive effects. Furthermore, no QTLs for anorexia or antibody response were detected despite large differences for these traits between the founder lines. The result is an excellent example where a large phenotypic difference between populations occurs in the apparent absence of any single locus with large phenotypic effects. The study underscores the need for powerful experimental designs in genetic studies of multifactorial traits. No QTL at all would have reached genome-wide significance using a less powerful design (e.g. approx. 200 F2 individuals) regardless of the nine-fold phenotypic difference between the founder lines for the selected trait.

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Corresponding author
Department of Medical Biochemistry and Microbiology, Uppsala University, BMC, Box 597, SE-75124 Uppsala, Sweden. Tel: +46 18 4714904. Fax: +46 18 4714833. e-mail: Leif.Andersson@imbim.uu.se
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Genetics Research
  • ISSN: 0016-6723
  • EISSN: 1469-5073
  • URL: /core/journals/genetics-research
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